If quality is a vital part of your DNA, and you have experience from working with packaging materials for pharmaceuticals, we have a very interesting job just waiting for you.
Broad and exciting responsibility for audits, agreements, projects etc.
As GMP Auditor you will take on a major responsibility in order to ensure that LEO Pharma have the best packaging materials in the right quality and at the right price. In overview your primary tasks will be to:
- plan and complete audits of packaging materials suppliers
- establish Quality Agreements with packaging materials suppliers
- perform regular evaluations of supplier quality performance
- participate in projects concerning new or changed packaging materials
- maintain and develop the QMS with focus on supplier interactions
- deliver quality support to our internal stakeholders regarding changes, complaints, SOP’s and quality issues
You can look forward to travelling a minimum of 20 days per year to meet colleagues, suppliers and partners (mainly within Europe).
+3 years’ pharma related experience including GMP-knowledge
Your theoretical background is a natural science degree at minimum B.Sc. level, e.g. pharmacy, engineering or chemistry. This is backed by minimum 3 years’ experience from working in the pharmaceutical industry or a supplier to pharmaceutical industry. As such, you have a strong knowledge of GMP and preferably also ISO standards for packaging material manufacturers. If you bring experience from performing audits it is a plus but experience from being audited can also be the starting point.
As you will be working in a truly global environment you must thrive on working together with people from different cultures, industries and professions. This takes an open and pragmatic attitude including the ability to understand a given situation from different angles. You find energy and motivation in developing solutions that make a real difference, no matter if it is a small optimisation of a process or the creation of a new super agreement.
Affiliates & External Suppliers Quality – your new department
You will join 15 enthusiastic colleagues located in Ballerup, Dublin and Parsippany. Our focus is to ensure second to none quality and compliance within LEO Affiliate Companies worldwide and at our third parties; including suppliers, contract manufacturers, contract laboratories and distributors. We establish quality agreements, perform audits and follow up on third party quality performance. We also participate in projects concerning new third parties and supply chain improvements. A vital part of our work is based on close collaboration with internal stakeholders across multiple departments within our supply chain. We are part of the Global Quality & EHS organization with a total of 170 employees worldwide.
We look forward to receiving your application.
